Affiliation:
1. Multidisciplinary Institute for Investigation in Pediatric Pathologies (IMIPP) CONICET‐GCBA, Molecular Biology Laboratory, Pathology Division, Ricardo Gutierrez Children's Hospital Buenos Aires Argentina
2. Pathology Division Marie Curie Hospital Buenos Aires Argentina
3. Pathology Division Ricardo Gutierrez Children's Hospital Buenos Aires Argentina
4. Hemathology Division Ricardo Gutierrez Children's Hospital Buenos Aires Argentina
5. Pathology Division Prof. Dr. Juan P. Garrahan Hospital Buenos Aires Argentina
Abstract
AbstractIn 2017, the World Health Organization (WHO) confirmed a new entity, Epstein Barr virus (EBV) + Diffuse large B cell lymphoma (DLBCL), not otherwise specified (NOS). Traces of EBV transcripts were described in lymphomas, including DLBCL, that were diagnosed as EBV negative by conventional methods. The aim of this study was to detect viral genome by qPCR, as well as LMP1 and EBNA2 transcripts, with a more sensitive method in DLBCL cases from Argentina. Fourteen cases originally considered as EBV negative expressed LMP1 and/or EBNA2 transcripts. In addition, LMP1 and/or EBNA2 transcripts were also observed in bystander cells. However, EBERs+ cells cases by conventional ISH showed higher numbers of cells with LMP1 transcripts and LMP1 protein. In the cases that were EBERS− in tumor cells but with expression of LMP1 and/or EBNA2 transcripts, the viral load was below the limit of detection. This study provides further evidence that EBV could be detected in tumor cells by more sensitive methods. However, higher expression of the most important oncogenic protein, LMP1, as well as increased viral load, are only observed in cases with EBERs+ cells by conventional ISH, suggesting that traces of EBV might not display a key role in DLBCL pathogenesis.
Funder
Consejo Nacional de Investigaciones Científicas y Técnicas
Fondo para la Investigación Científica y Tecnológica
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1 articles.
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